Pharma Manufacturing Technician

Biopharma Careers; United States; On-site; USD 34,000 - 52,000; Full time

Benefits offered by this job

Total Rewards

Job summary

Perrigo is hiring for a manufacturing roles focused on operating equipment and maintaining quality in a fast-paced environment. You will record data, perform setup/changeovers, and ensure compliant paperwork under cGMP/SOP guidelines.

Candidates should have a high school diploma, basic math and reading skills, and be able to work overtime as required. Prior pharma/FDA-regulated experience is a plus.

Qualifications

• High School Diploma or Equivalency required.
• Basic math and reading comprehension skills; able to read, speak, and comprehend English instructions and proofread alpha/numeric data.
• Must follow Standard Operating Procedures (SOPs).
• Basic computer skills and ability to navigate training systems as part of daily work.
• Able to communicate effectively as a team member.
• Must meet locally defined training requirements.
• Experience in a pharmaceutical or FDA-regulated environment is preferred.
• Must operate and handle material handling equipment.
• Ability to work overtime as required.

Responsibilities

• Operates and ensures proper operation of manufacturing equipment.
• Conducts regular in-process checks of quality attributes of materials and products to ensure equipment is operating correctly.
• Records accurate production and inspection data and completes manufacturing paperwork per SOPs and cGMPs.
• Performs set ups, changeovers and cleans the work area during the shift to maintain proper material clearance.
• Suggests and participates in process, productivity and quality improvements to reduce costs.
• Performs other related duties as assigned.

Skills

Basic math

Reading comprehension

English proficiency

Teamwork

Communication

Computer skills

Education

High School Diploma or Equivalency

Tools

Computer skills

Job description

Perrigo is hiring for a manufacturing roles focused on operating equipment and maintaining quality in a fast-paced environment. You will record data, perform setup/changeovers, and ensure compliant paperwork under cGMP/SOP guidelines.

Candidates should have a high school diploma, basic math and reading skills, and be able to work overtime as required. Prior pharma/FDA-regulated experience is a plus.